Canonical Allele Identifier: CA2761703082

Gene: KIT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.54727422_54727423insAACACACCCAACACA , CM000666.2:g.54727422_54727423insAACACACCCAACACA	GRCh38
NC_000004.11:g.55593588_55593589insAACACACCCAACACA , CM000666.1:g.55593588_55593589insAACACACCCAACACA	GRCh37
NC_000004.10:g.55288345_55288346insAACACACCCAACACA	NCBI36
NG_007456.1:g.74428_74429insAACACACCCAACACA , LRG_307:g.74428_74429insAACACACCCAACACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412167.7:c.1645_1646insAACACACCCAACACA	ENSP00000390987.3:p.Pro548_Met549insLysHisThrGlnHis
ENST00000685269.1:n.1732_1733insAACACACCCAACACA
ENST00000686011.1:c.1642_1643insAACACACCCAACACA	ENSP00000509704.1:p.Pro547_Met548insLysHisThrGlnHis
ENST00000687109.1:c.1657_1658insAACACACCCAACACA	ENSP00000509371.1:p.Pro552_Met553insLysHisThrGlnHis
ENST00000687208.1:n.2069_2070insAACACACCCAACACA
ENST00000687246.1:c.1642_1643insAACACACCCAACACA	ENSP00000509114.1:p.Pro547_Met548insLysHisThrGlnHis
ENST00000687265.1:n.1812_1813insAACACACCCAACACA
ENST00000687295.1:c.1642_1643insAACACACCCAACACA	ENSP00000509450.1:p.Pro547_Met548insLysHisThrGlnHis
ENST00000689832.1:c.1657_1658insAACACACCCAACACA	ENSP00000509084.1:p.Pro552_Met553insLysHisThrGlnHis
ENST00000689994.1:c.1144_1145insAACACACCCAACACA	ENSP00000509156.1:p.Pro381_Met382insLysHisThrGlnHis
ENST00000690543.1:c.1645_1646insAACACACCCAACACA	ENSP00000508831.1:p.Pro548_Met549insLysHisThrGlnHis
ENST00000690917.1:n.1872_1873insAACACACCCAACACA
ENST00000691361.1:n.564_565insAACACACCCAACACA
ENST00000692783.1:c.1654_1655insAACACACCCAACACA	ENSP00000508733.1:p.Pro551_Met552insLysHisThrGlnHis
ENST00000692991.1:n.1751_1752insAACACACCCAACACA
ENST00000288135.6:c.1654_1655insAACACACCCAACACA MANE Select	ENSP00000288135.6:p.Pro551_Met552insLysHisThrGlnHis
ENST00000288135.5:c.1654_1655insAACACACCCAACACA	ENSP00000288135.5:p.Pro551_Met552insLysHisThrGlnHis
ENST00000412167.6:c.1642_1643insAACACACCCAACACA	ENSP00000390987.2:p.Pro547_Met548insLysHisThrGlnHis
NM_000222.2:c.1654_1655insAACACACCCAACACA , LRG_307t1:c.1654_1655insAACACACCCAACACA	NP_000213.1:p.Pro551_Met552insLysHisThrGlnHis
NM_001093772.1:c.1642_1643insAACACACCCAACACA	NP_001087241.1:p.Pro547_Met548insLysHisThrGlnHis
XM_005265740.1:c.1657_1658insAACACACCCAACACA	XP_005265797.1:p.Pro552_Met553insLysHisThrGlnHis
XM_005265741.1:c.1657_1658insAACACACCCAACACA	XP_005265798.1:p.Pro552_Met553insLysHisThrGlnHis
XM_005265742.1:c.1645_1646insAACACACCCAACACA	XP_005265799.1:p.Pro548_Met549insLysHisThrGlnHis
XM_005265742.3:c.1645_1646insAACACACCCAACACA	XP_005265799.1:p.Pro548_Met549insLysHisThrGlnHis
XM_017008178.1:c.1654_1655insAACACACCCAACACA	XP_016863667.1:p.Pro551_Met552insLysHisThrGlnHis
XM_017008179.1:c.1645_1646insAACACACCCAACACA	XP_016863668.1:p.Pro548_Met549insLysHisThrGlnHis
XM_017008180.1:c.1642_1643insAACACACCCAACACA	XP_016863669.1:p.Pro547_Met548insLysHisThrGlnHis
NM_000222.3:c.1654_1655insAACACACCCAACACA MANE Select	NP_000213.1:p.Pro551_Met552insLysHisThrGlnHis
NM_001093772.2:c.1642_1643insAACACACCCAACACA	NP_001087241.1:p.Pro547_Met548insLysHisThrGlnHis
NM_001385284.1:c.1657_1658insAACACACCCAACACA	NP_001372213.1:p.Pro552_Met553insLysHisThrGlnHis
NM_001385285.1:c.1654_1655insAACACACCCAACACA	NP_001372214.1:p.Pro551_Met552insLysHisThrGlnHis
NM_001385286.1:c.1642_1643insAACACACCCAACACA	NP_001372215.1:p.Pro547_Met548insLysHisThrGlnHis
NM_001385288.1:c.1645_1646insAACACACCCAACACA	NP_001372217.1:p.Pro548_Met549insLysHisThrGlnHis
NM_001385290.1:c.1657_1658insAACACACCCAACACA	NP_001372219.1:p.Pro552_Met553insLysHisThrGlnHis
NM_001385292.1:c.1645_1646insAACACACCCAACACA	NP_001372221.1:p.Pro548_Met549insLysHisThrGlnHis